Rubber compositions containing silica and an organosilane

ABSTRACT

Sulfur containing organosilicon compounds having the formula:

Unite States Patent [191 Thurn et al.

[ Mar. 25, 1975 1 RUBBER COMPOSITIONS CONTAINING SILICA AND AN ORGANOSILANE [75] inventors: Friedrich Thurn, Bruhl; Kurt Burmester, Overath-Steinenbruck; Johannes Pochert, Walberberg; Siegfried Wolff, Bruhl, all of Germany [73] Assignee: Deutsche Goldund Silber-Scheideanstalt vormals Roessler, Frankfurt am Main, Germany [22] Filed: Nov. 12, 1973 [21] Appl. No.: 415,176

Related U.S. Application Data [63] Continuation-impart of Ser. No. 277,043, Aug. 1,

1972, Pat. N0. 3,842,111.

[30] Foreign Application Priority Data Aug. l7, 197] Germany "2141 159 Nov. l3, 1972 Germany 2255577 [56] References Cited UNITED STATES PATENTS v 3,768,537 l0/l973 Hess et ul. 260/4l.5 A

Primary Examiner-Donald E. CZzlja Assistant ExaminerH. H. Fletcher Attorney, Agent, or FirmCushman, Darby & Cushman [57] ABSTRACT Sulfur containing organosilicon compounds having the formula:

in which Z is:

R R R 1 r 1 2 sK-R SR or Si--R where R is alkyl of l to 4 carbon atoms cyclohexyl or phenyl and R is alkoxy of l to 8 carbon atoms, cycloalkoxy of 5 to 8 carbon atoms or alkylmercapto of l to 8 carbon atoms, alk of a divalent aliphatic hydrocarbon or unsaturated aliphatic hydrocarbon or a cyclic hydrocarbon containing 1 to 18 carbon atoms and n is a whole number from 2 to 6 are used as reinforcing additives in rubber mixtures containing a silica or silicate filler, and in a given case carbon black; the or ganosilane is coated on the surface of the silica 0r silicate filler particles.

31 Claims, No Drawings RUBBER COMPOSITIONS CONTAINING SILICA AND AN ORGANOSILANE This application is a continuation-in-part of application Ser. No. 277,043 filed Aug. 1, 1972, now U.S. Pat. No. 3,842,111.

The present invention is directed to additives for silicate or silica filler containing rubber mixtures which additives favorably influence the production of the rubber mixtures and the properties of the vulcanizate in a surprising and decisive manner. These additives belong chemically to the group of organosilicon compounds containing sulfur in the molecule. The additives impart to the silica (or silicate) fillers improved reinforcing properties and increase the over-all cross-linking of the vulcanization; they are designated as reinforcing additives in the following description.

It is known that carbon blacks generally, and especially the especially developed types of carbon black, are not present merely as fillers in rubber vulcanizate but take part in a specific manner as reinforcing fillers (active fillers). The influence of carbon black on the reinforcement of the polymers and the determination of the rubber-filler-reciprocal effect are described for example in the magazine Kautschuk und Gummi, Kunstoffe", No. 8, pages 470-474 (1966) and No. 1, pages 7l4 (1970).

The silica (or silicate) fillers, i.e., siliceous materials as, for example, highly dispersed silica, silicates or the like are known to be different in their activity from carbon blacks. This difference is recognized by two kinds of facts. First the reinforcing effect of silica or silicate fillers is different from that of carbon black because of their completely different type of surface. Secondly, the active silica influence the vulcanization process, especially if the vulcanization is effected by sulfur and accelerator additives. Previously there have been no sulfur vulcanizations in which the silica (or silicate) fillers did not reduce the cross-linking.

In recent years there have been attempts to improve the activity of silica (or silicate) fillers by admixing chemical substances to the starting mixture.

Thus it is known to use mercaptomethylalkoxysilane as an adhesive promoter between silicate materials such as glass, clay, asbestos and silica dioxide (silica) and organic resins such as butadiene-styrene copolymers, natural rubber, polyester resins, polystyrene and styrene-maleic anhydride-mixed polymers, whereby this silane is introduced on the substrate in any desired manner and bound with the resin, see German Offenlegungsschrift No. 2,038,715.

Furthermore, there are known organosiliconsulfide compounds having a sulfidic sulfur atom between the hydrocarbon radicals which are recommended for use as adhesive promoters or also as intermediate products for compounds which can be used as water repelling agents or oxidizing agents. The named organosilicon compounds, however, can also have sulfur containing end groups such as thiocyanato, xanthogenato, thioether, thionic acid ester groups or the like, see Lee, German Auslegeschrift No. 1,911,227.

The organo-organooxysilanes, for example, the 3- thiocyanatopropyl-trimethoxyor triethoxysilane, which according to Belgian Pat. No. 770,097 and Rocktaschel U.S. application Ser. No. 163,467 filed July 16, 1971 find outstanding use in cross-linkable or vulcanizable mixtures of organic polymers, inorganic materials and the corresponding cross-linking or vulcanization agents or systems have similar end groups. The silanes described in German Auslegeschrift No. 1,911,227, Belgian Pat. No. 770,097 and the Rocktaschel U.S. application possess only a silicon atom bound to a carbon atom or a further silicon atom bound thereto by an oxygen atom or an amino nitrogen atom.

Furthermore there are known gamma-mercaptopropyl-trimethoxy and triethoxy silanes as well as beta-mercaptoethyl-triethoxy silane and other sulfur .free silanes, which after subsequent partial hydrolysis and coating on the surface of silica or silicate filler particles serve to facilitate the workability of rubber mixtures and improvement of the strength properties of reinforced rubber articles, Vanderbilt U.S. Pat. No. 3,350,345.

Besides there are known tire threads produced form a rubber mixture which contain a silica as a filler and a silane as coupling agent, see Belgian Pat. No. 760,099. An exceedingly large number of silanes are included in the general formula in the Belgian patent, but from the introduction, the tables and examples there can only be found gamma-mercaptopropyltrimethoxysilane as the single coupling agent tried.

The present invention is drawn to a class of organosilanes containing sulfur in the molecule which are distinguished in several respects from the numerous known silanes in their outstanding advantages in use and especially in their suitability and reinforcing additives as is described and shown below. The new additives produce in siliceous fillers (i.e., silica and silicates) containing rubber mixtures and vulcanizates unforeseen, valuable and industrially outstanding properties, whereby the rubber mixtures contain at least one rubber, a cross-linking system (e.g., including sulfur), a sulfur containing organosilane, fillers and preferably further conventional rubber additives. The invention is characterized by the rubber mixture containing as a strengthening additive one or more organosilanes of the formula:

I ZalkS,,-alk-Z in which Z is:

- $1 11 Six-R or 51 R and in which R, is an alkyl group of l to 4 carbon atoms or phenyl and R is analkoxy group with l to 8, preferably 1 to 4, carbon atoms, a cycloalkoxy group with 5 to 8 carbon atoms or a straight or branched chain alkylmercapto group with 1 to 8 carbon atoms. All the R and R groups can be the same or different. Alk is a divalent hydrocarbon group with 1 to 18 carbon atoms. It can be straight or branched chain and can be a satu' rated aliphatic hydrocarbon group, an unsaturated aliphatic hydrocarbon group or a cyclic hydrocarbon group. Preferably alk has 1 to 6, most preferably 2 or 3 carbon atoms and n is a [whole] number of 2 to 6, as well as one or more siliceous fillers (i.e. silica or a silicate), in a given case in admixture with carbon black. Preferably n is 2 to 4, more preferably 3 to 4.

Preferably the rubber mixtures contain at least one organosilane, especially one or two, most preferably one, of formula I in which Z stands for the group R2 H II R s1 Alk s Alk Si -R: R \R2 where R is OCH -OCH-,CH OCH CH CH strength, abrasion resistance, rebound and shore hardness of the vulcanizate.

On the contrary, however, the scorch time and the Defo-elasticity of the unvulcanized mixtures are influenced unfavorably. The scorch times are shortened drastically. In the production of such mixtures even in the internal mixer frequently there occurs premature scorching which makes it impossible to further work the mixture.

The Defo-elasticity is sharply increased which means an increase of the elastic rubber portion in the crude mixture and makes more difficult the further processing, for example, by extrusion.

On the contrary, the rubber mixtures containing the new reinforcing additives employed in the present invention show definite industrial advantages in regard to the properties of the raw mixtures and the vulcanizates in comparison to those in the art. The raw mixtures now show especially a previously unknown degree of processing safety, a strongly reduced stiffness and only a slight increase of Defo-elasticity. All of these advantageous properties or effects for the first time open up the industrial use of such mixtures. The properties of the vulcanizates obtained are excellent and are compaand OCH(CH )CH Alk is -CH CH CH -C JH-; CH2 ca 011 CH- CH3 CH2 J CH2CH2()H CH2- and -cH cH cH- and CH CH3 and n is 2.0 to 4.0 Other preferred silanes are those wherein in place of Si--R in formula I, Z can be 1 1 $1 12 or Si R wherein R is alkyl (branched or unbranched with l to 4 carbon atoms), phenyl or cyclohexyl and R is as defined for formula ll.

The new silanes used in the invention also have in the middle of the somewhat symmetrical molecule two or more connected sulfur atoms and two separated, to a certain degree, terminal standing silane groups. It must be accepted that this molecular structure causes the outstanding properties of the new vulcanization reinforcer.

The 3-mercaptopropyltrimethoxysilane already mentioned above in rubber mixtures which contain silica as a filler definitely increases the modulus values, tensile err-ca is 2.0 to h.o

rable with the properties of correspondingly carbon black filled vulcanizates or even exceed these, as will be pointed out below. The mentioned improvement of the properties of the raw mixture and the vulcanizate for the first time opens field of use of silica fillers which previously were reserved for only carbon black as reinforcing filler.

The term siliceous filler is a broad term and refers to fillers which are rubber compatible or can be worked into rubber mixtures which fillers consist of silicates or silica, or contain silicates or silica and/or contain chemically bound silicates (or silica) in the widest sense, including mixtures of two or more siliceous fillers. Especially counted as siliceous fillers are:

Highly dispersed silica (silicon dioxide) having a specified surface area in the range of about 5 to 1000, preferably 20 to 400 m /g (determined with gaseous nitrogen according to the known BET procedure) and with primary particle sizes in the range of about 10 to 400 nm. (nanometer, 10" meters), which can be produced, for example, by precipitation from solutions of silicates, by hydrolysis and/or oxidative high temperature conversion. There can also be used flame hydrolysis of volatile silicon halides, e.g., silicon tetrachloride, or by electric arc processes. These silicas, in a given case, can also be present as mixed oxides or oxide mixtures with oxides of the metals aluminum (alumina), magnesium (magnesium oxide), calcium (calcium oxide), barium (barium oxide), zinc (zinc oxide), zirconium (e.g., zirconium dioxide), or titanium (e.g., titanium dioxide).

Synthetic silicates, for example, aluminum silicate or alkaline earth silicates such as magnesium, or calcium silicate with specific surface areas of about 20 to 400 m /g and primary particle sizes of about to 400 nm.

Natural silicates, for example, kaolin, wollastonite, talc and asbestos as well as natural silicas, e.g., quartz or sand.

Glass fibers and glass fiber products such as mats, webs, strands, fabrics, non-woven fabrics and the like as well as microglass balls (microglass balloons).

The siliceous fillers mentioned can be added in amounts of about 10 or, in a given case, even less, up to about 250 parts by weight based on 100 parts by weight of rubber polymer.

As filler mixtures there can be used, for example, silica-kaolin or silica-glass fibers-asbestos, as well as blends of siliceous reinforcing fillers with the mentioned rubber blacks, for example, silica-ISAF carbon black or silica-glass fiber cords l-lAF carbon black.

Typical examples of siliceous fillers usable in the invention, for example, are those produced by Degussa, such as silica or silicates under the tradenames; Aerosil, Ultrasil, Silteg, Durosil, Extrusil, Calsil, etc.

Furthermore there can be mixed into the rubber mixtures various additives which are well known in the rubber industry and widely used.

There are several advantages if the additive of the invention is not added as such to the rubber mixture but first a mixture of at least on siliceous filler and at least one organosilane of formula 1 above is prepared and this is then or later incorporated in the rubber mixture of the remaining components of the mixture of the rubber mixture in the customary manner with the help of conventional mixing apparatus and homogeneously distributed therein.

In the production of the master batch, there is still a fluid, dry product if there is mixed into the siliceous filler an equal or even larger amounts by weight of liquid organosilane. Consequently, it is also possible to add only a portion of the entire fillers needed to produce the rubber mixture which as a master batch already contains the entire amount of necessary silane.

Examples of organosilanes within formula I which can be used in the invention are bis[trialkoxysilyl-alkyll )l-polysulfides such as bis[2-trimethoxy-, -triethoxy-, -tri-(methylethoxy)-, -tripropoxy-, -tributoxy and so forth up to -trioctyloxysilyl-ethyl]-polysulfides, namely the di-, tri-, tetra-, penta-, and hexasulfides, further the bis-[3-trimethoxy-, -triethoxy-, -tri-(methylethoxy)-, -tripropoxy-, -tributoxyand so forth up to -trioctoxypropyll-polysulfide, namely again the di-, tri-, tetra-, pentaand hexasulfide; furthermore the corresponding bis[3-trialkoxysilylisobutyl]- polysulfides, the corresponding bis[4-trialkoxysilyl-butyl1- polysulfides and so forth up to bis[6-trialkoxysilyl-hexyl]-polysulfides. Of those chosen, there are preferred relatively simply constructed organosilanes of formula I including bis- [3-trimethoxy-, -triethoxy-, and -tripropoxysilylpropyl]- polysulfides namely the di-, triand tetrasulfides. These and the other organosilanes of formula I which can be added with good success can be made ac cording to the process of Meyer-Simon application Ser. No. 277,043 filed on Aug. 1, 1973 which corresponds to German patent applications P 21411596; P 21411609 and P 22122399. The entire disclosure of Meyer-Simon (and the corresponding German applications) is hereby incorporated by reference. Typical examples of specific compounds within the formula 1 which can be used in the invention include:

Examples of compounds within the invention include 3,3 '-bis (trimethoxysilylpropyl) disulfide, 3,3 -bis (triethoxysilylpropyl) tetrasulfide, 3,3-bis(trimethoxysilylpropyl) tetrasulfide, 2,2'-bis (triethoxysilylethyl) tetrasulfide, 3,3-bis (trimethoxysilylpropyl) trisulfide, 3,3- bis (triethoxysilylpropyl) trisulfide, 3,3'-bis (tributoxysilylpropyl) disulfide, 3,3'-bis(trimethoxysilylpropyl) hexasulfide, 3,3'-bis(trioctoxysilylpropyl) tetrasulfide, 3,3-bis(trihexoxysilylpropyl) disulfide, 3,3-bis(tri-2"- ethylhexoxysilylpropyl) trisulfide, 3,3-bis(triisooctoxysilylpropyl) tetrasulfide, 3 ,3 '-bis(tri-tbutoxysilylpropyl) disulfide, 2,2'-bis(methoxy diethoxy silyl ethyl) tetrasulfide, 2,2-bis (tripropoxysilylethyl) pentasulfide, 3,3'-bis (tricyclohexoxysilylpropyl) tetrasulfide, 3,3-bis(tricyclopentoxysilylpropyl) trisulfide, 2,2-bis(tri-2"-methylcyclohexoxysilylethyl) tetrasulfide, bis(trimethoxyxilylmethyl) tetrasulfide, 3,3'-bis (trimethylmercaptosilylpropyl) tetrasulfide, 2,2'- bis(triethylmercaptosilylethyl) disulfide, 2,2'- bis(tributylmercaptosilylethyl) trisulfide, 2,2'-bis(tri sec. butylmercaptosilylethyl) trisulfide, 3,3'-bis (trioctylmercaptosilylpropyl) tetrasulfide, 2,2-bis (trihexylmercaptosilylethyl) hexasulfide, 3,3'-bis (ethyldipropylmercaptosilylpropyl) tetrasulfide, 3-methoxy ethoxy propoxysilyl 3'-diethoxybutoxysilylpropyltetrasulfide, 2,2-bis (dimethyl methoxysilylethyl) disulfide, 2,2'-bis(dimethyl sec.but0xysilylethy1) trisulfide, 3,3'- bis (methyl butylethox'ysilylpropyl) tetrasulfide, 3,3'- bis(di-t-butylmethoxysilylpropyl) tetrasulfide, 2,2'-bis (phenyl methyl methoxysilylethyl) trisulfide, 3,3'-bis (diphenyl isopropoxysilylpropyl) tetrasulfide, 3,3- bis(diphenyl cyclohexoxysilylpropyl) disulfide, 3,3'- bis(dimethyl ethylmercaptosilylpropyl) tetrasulfide, 2,2'-bis(methyl dimethoxysilylethyl) trisulfide, 2,2'- bis(methyl ethoxypropoxysilylethyl) tetrasulfide, 3,3'- bis(diethyl methoxysilylpropyl) tetrasulfide, 3,3'-bis (ethyl di-sec. butoxysilylpropyl) disulfide, 3,3- bis(propyl diethoxysilylpropyl) disulfide, 3,3 '-bis(butyl dimethoxysilylpropyl) trisulfide, 3,3-bis(phenyl dimethoxysilylpropyl) tetrasulfide, 3-phenyl ethoxybutoxysilyl 3'-trimethoxysilylpropyl tetrasulfide, 4,4- bis(trimethoxysilylbutyl) tetrasulfide, 6,6'-bis (triethoxysilylhexyl) tetrasulfide, l2,l2'-bis(triisopropoxysilyl dodecyl) disulfide, 18,18- bis(trimethoxysilyloctadecyl )tetrasulfide, 18,18 '-bis (tripropoxysilyloctadecenyl) tetrasulfide, 4,4- bis(trimethoxysilyl-buten-Z-yl) tetrasulfide, 4,4'-bis (trimethoxysilylcyclohexylene) tetrasulfide, 5,5 bis(dimethoxy methylsilylpentyl) trisulfide, 3,3'-

bis(trimethoxysilyl-Z-methyl propyl) tetrasulfide, 3,3- bis(dimethoxyphenylsilyl-2-methylpropyl) disulfide.

The new silanes used in the invention can be added to the rubber mixture in amounts of 0.1 to 50 parts by weight, preferably within the limits of 0.5 to 25 parts by weight based on parts by weight of rubber.

Unless otherwise indicated all parts and percentages are by weight.

For use the organosilanes described above can be directly added to the rubber mixture or to the constituents of this mixture. Thereby it is not necessary and not advantageous to hydrolyze the organosilane before the addition.

However, the described organosilicon compounds can also be added to a part of the fillers, especially on the basis of their easy dosability and handling, whereby the liquid organo-silane is converted into a powdery product and thus be used. In a given case, however, it is also possible, although not of special advantage, to uniformly coat the organosilane on the surface of the filler particles and in the form to carry out the use. All three or only two of the described methods of use can also be combined.

The rubber mixture can'be produced with one or more, in a given case oil-extended, natural and/or synthetic rubbers. These include especially natural rubber, synthetic rubbers, preferably diene elastomus as for example polybutadiene, polyisoprene, e.g., cispolyisopre'ne, butadienestyrene copolymer, butadienc-acrylonitrile copolymer, polymerized 2- chlorobutadiene, also butyl rubber, halogenated butyl rubber such as chlorinated butyl rubber, brominated butyl rubber as well as other known diene rubbers as for example terpolymers of ethylene, propylene and for example non-conjugated dienes and also nonconjugated polyenes, e.g., ethylene-prpoylenecyclooctadiene, ethylene-propylene-norbornadiene, ethylene-propylene dicyclo-pentadiene and ethylenepropylene-cyclododecatriene. Also there can be used trans-polypentenamer, carboxy or epoxy rubbers and the like known elastomers. The chemical derivatives of natural rubber and modified natural rubber can also be used in the invention.

procedures system the rubber industry.

Industrial fields of use for the described rubber mixtures for example are:

Industrial rubber articles such as cable insulation, hoses, driving belts, V-belts, conveyor belts, roller coating, vehicle tire treads, especailly PKW and LKW- tire treads, as well as tire carcasses and tire sidewalls, cross country tires, shoe sole materials, packing rings, damping elements and many others. The new rubber mixtures have also been tested for glass fiber-adhesive mixtures and the like.

The filler Ultrasil VN2 is precipitated active silica having a specific surface area (measured according to BET) of I m t /g and an average primary particle size of 28 nm.

The Ultrasil VN3 is likewise a precipitated active silica but has a specific surface area of 210 m /g and an average primary particle size of 18 nm.

The rubber Buna C810 is a polybutadiene rubber having a high cis-l,4- content.

Russ Corax 6LM is a ISAF-active carbon black wherein the large characters LM is an abbreviation for Low Modulus.

Without limiting the invention the results are given in the following individual recipes for the new rubber mixtures with test results on the vulcanizates and evaluations or comparisons of these results. Therein many different concepts are repeated so that abbreviations can be used.

Definitions of the Abbreviations Used Flexometer) C There can be added, in a given case, to the rubber mixtures of the organic polymers, the cross-linking systems, the siliceous fillers and the organosilane additive known reaction accelerators, as well as one or more compounds of the group of antiaging agents, heat stabilizers, light stabilizers, ozone stabilizers, processing aids, plasticizers, tackifier, propellants, dyestuffs, pigments, waxes, extenders such as for example sawdusts, organic acids as for example stearic acid, benzoic acid, or salicyclic acid, additionally lead oxide or zinc oxide, activators such as for example triethanolamine, polyethylene glycol or hexanetriol-l,2,6, which are collectively known in the rubber industry. For the vulcanization the rubber mixture is generally mixed with crosslinking agents such as especially peroxides, e.g, benzoyl peroxide, sulfur or in special cases magnesium oxide, as well as in a given case vulcanization accelerators or mixtures of these.

The production of rubber mixtures as well as molding and vulcanization is carried out according to customary TESTING STANDARDS The physical tests were carried out at room temperature according to the following standard specifications:

(DIN German industrial standards) Tensile strength, elongation at break and The vulcanizates were always produced in a steam heated multiple die press at the stated vulcanization temperatures.

In the examples, and elsewhere unless otherwise indicated all amounts of materials are always given in parts by weight.

Example i Example Z-Continued Mixture Mixture Mixture Mixture Mixture Mixture Recipe: 1 2 3 Rfgclpei y l 2 3 Natural rubber 5 Zinc oxide (active) 2 2 2 (Ribbed Smoked Sheets I) lOO I I00 Antioxidant (Mixture of Pentachlorthio hen l-zinc aralkylated Phenol i l 1 salt (Renacit V o Mixture of equal parts of Farhcnfahriken BAYER) 0.25 0.25 0.25 finely divided precipitat- Finely divided preeipied silica and hexunetriol titled silica (L ltrnsil l0 (Aktivutor R of DEGUSSA) 4 4 4 VN 3 of Degussu) 40 40 40 Benzoic acid 0.8 0.8 0.8 Zinc oxide 3 3 3 3-Mercuptopropyl- Steuric acid 2 2 2 trimethoxystlune 1.5 3-tnereuptopropyl- Bis-l3-triethoxysil ltrimethoxysilane 2 propyll-tetrasulfi e 1.5 Bis-l 3-trimcthoxysilyl- Dibcnzothiazyldisulfidc 0.8 0.8 0.8 propyll-trisulfide 2 l5 Diphenylguanidine 1.6 1.6 1.6 Dibenzothiazyldisulfidc 0.8 0.8 0.8 $11 fur 2.5 2.5 2.5 Diphenylguanidine 2.25 2.25 2.25 Sulfur 2.5 2.5 2.5

Mixing Procedure Mixing Procedure Premixing in a kneader at 80C. flow temperature.

Preliminary mixing was in a kneader at 80C. flow temperature Additive or Treatment E d d Aft r Additive or Treatment Ended After Natural rubber 0 min t cis-l.4-Polyis0prene rubber 0 minutes /1 the amount of sili /2 amount of silica, stearic acid 1 minute stearic acid 1 minute amount of silica, plasticizer, h amount f ili zinc oxide, organosilane 2.5 rninutes zinc oxide and organosilane 2.5 minutes Ram lifted and Swep down 4 mmlnes Ram lifted and swept down 4 minutes Bmch dumped mmuws Batch dumped 4.5 minutes This mixture was allowed to be stored for 24 hours. Af r tanding for 24 hours final mixing was accom- Then the final mixing took place in the kneader at plished at 80C. flow temperature in a kneade 80C. flow temperature (Mixing Time 1.5 minutes). 5 g minutes)- Propcrties of the unvulcanized mixtures Mixture l Mixture 2 Mixture 3 DH/DE 675/20 precured 650/20 (scorched) 6.4 v 5.0 I 7.5 5.8 ML 4 57 232 (increas- 54 ing) sp.gr. L13 L13 l.l3

Properties of the vulcanized Mixture vulcanization tem eruture: 150C. Mixture Z 300 BD bl.D E SH EF A i 10 256 62 622 41 50 62 39 20 250 58 630 43 47 64 3! 229 48 640 37 46 62 35 I65 60 227 42 678 33 62 35 2 10 20 40 3 I0 274 558 41 47 63 27 20 257 94 548 36 48 64 29 40 262 84 580 35 48 6l' 25 I40 60 242 76 582 28 47 61 27 Example 2 60 Properties of the unvulcanized mixtures Recipe: Mixture Mixture Mixture l 2 3 Mixture l Mixture 2 Mixture 3 i l 4 P i DH/DE [SOD/6.0 scorched l375/7.0 rub r I00 I00 5 9.2 6.5 finely divided, precipi t l L6 8A tated silica (ULTRASIL 65 ML 4 100 154 91 VN 3 of DEGUSSA) 5O 50' 50 (increasing) Plasticizer (naphthenic P- gl'. 1.l3 1.14 1.14 hydrocarbons) 3 3 3 Properties of the vulcanized Mixture vulcanization temperature: 134T. Mixture Z Z M 300 BD hl.D E SH EF A 1 I I36 21 707 I7 33 48 I 20 v 242 63 640 3l 42 68 44 I58 30 266 79 628 36 43 7l 4! 40 272 87 620 4! 44 72 43 ln examples 1 and 2 there were used a rubber mixture based on natural rubber or synthetic cis-l,4- polyisoprene which contained as the siliceous filler a precipitated finely divided silica (Ultrasil VN 3 of Degussa). As reinforcing additive for the rubber mixture there were employed bis-[3-trimethoxysilyl propyl]-trisulfide or bis-[3-triethoxysilyl tetrasulfide and 3-mercaptopropyl trimethoxysilane was employed as a comparison material of the prior art. As is already shown by the properties of the unvulcanized mixture in producing mixtures in the internal mixer only the raw rubber mixtures of the invention are able to be worked up further while the comparison mixtures could not be further worked because of the premature scorching.

The polysulfide organosilanes of the invention only shorten the scorching time t and 1 a short time in the mixtures and do not negatively effect the Mooney'plasticity (ML 4) as well as the ratio DH/DE, if the mixtures with the organosilane additives are compared with the standard or reference mixtures.

The vulcanization properties of the new rubber mix tures are, compared to the silane free standard mixtures, are somewhat better in their resistance and clearly superior in regards to 300 Modulus, whereby the reinforcing effect which is produced by the invention is proven by numerical data. The named important advantages were produced by means of the added organosilane.

Mixture 3 of example 2 additionally also shows extraordinarily high tear propagation resistance values (tear propagation resistance).

Example 3 Mixture l Mixture 2 p py l Mixing Procedure Premixing in a kneader at C. flow temperature.

Additive or Treatment Ended after l minute 2.5 minutes 4 minutes 4.5 minutes Accelerator and sulfur were mixed in on the rolls (Mixing time 1.5 minutes).

Properties of the unvulcanized mixtures Mixture l Mixture 2 Mixture 3 ML 196 tincreassp. gr. ,7 L16 Mixture 3 13 14 Properties of vulcanized mixtures Vulcunizntion tem eruturc: 150C. Mixture V7. 7. M 300 Ed hl.D E SH EF A l S 127 39 (ill) [9 47 58 5 I I40 40 630 ll 47 58 4 15 H6 4] 690 ill 47 58 160 20 Ill 4i 583 I6 47 58 4 2 8 l0 i5 20 3 X I42 78 560 I5 50 59 6 l0 l4() 6) 528 I3 50 59 5 I5 I30 7| 465 ll Si 60 4 I32 211 I21 72 500 l3 5] 60 5 Example 4 Example 5 Recipe: Mixlture Mixzture Mix3ture Recipe: Mixture Mixture Mixture Styrenc-Butadienc-rubbcr Styrene-Butadiene-rubber (Bunu Huls 1502) I00 I00 100 (Buna Huls 1500) 100 100 100 Finely divided. precipitated Colloidalkaolin 75 75 75 silica (ULTRASlL VN 3 of Zinc oxide 4 4 4 DEGUSSA) 5O 5O 50 Stearic acid 2 2 2 Zinc oxide (active) 1 l l 3-mercaptopro yl- Stcaric acid 2 2 2 trimethoxysi ane 2.5 Antioxidant-(mixture of Bis-[3-triethoxysilyluralkylutcd phenols) l I l propyl]-tetrasulfide 2.5 Polyethylene glycol. molecular Dibenzothiazyldisulfide L2 L2 l.2 wt. 4000 (PEG 4000) 2 2 2 Diphenylguanidine 1.2 1.2 1.2 3-mcrcuptopropyl- Sulfur 2.75 2.75 2.75 trimcthoxysilunc 2 Bis-[B-trimethoxysilylpropyl l-tlisulfidc 2 Dihcnzothiuzyldisulfidc l l l Diphcnylguanidine 2 2 2 Mlxlng Procedure 2 2 2 Prem1xing 1n a kneader at 80C. flow temperature.

Mlxmg Procedure Premixing 1n a kneader at 80C. flow temperature.

Additive or Treatment Ended After Additive or Treatment Ended After Rubber 0 minutes '72 amount of Kaolin, zinc oxide, Polymer (5BR) 0 minutes organosilane 2.5 minutes 4 amount of silica, stearic acid, Ram lifted and swept down 4 minutes antioxidant 1 minute Batch dumped 4.5 minutes amount of silica, zinc oxide, 40

organosilane, other 2.5 minutes Ram lifted and swept down 4 minutes Butch dumped 4.5 minutes time 1.5 minutes).

Properties of the unvulcanized mixtures ing time 1.5 minutes).

Mixture l Mixture 2 Mixture 3 Properties of the unvulcanized mixtures Mixture l Mixture 2 Mixture 3 D DE 2250 .5 h d 2050 3|.0 Bil i e Q; 011/012 1750/27 2550/325 1450/23.5 a 10.0 9.6 5 34.0 6.6 59.2 4 116 1.. 41.3 11.6 8.2 ML 4 143 2 2 grirgreas 's [7L 4 63 80 61 S gr. 1.16 1.16 g 1.17 P-g I32 2 1.32

Properties of the vulcanized mixtures vulcanization temgcruturc: 150C. Mixture vz F M 300 BD hl.D E SH EF A l 5 I 40 660 40 33 7] l7 10 174 42 640 34 33 72 l4 I5 I78 4l 625 3] 33 7] l3 l26 20 I96 42 647 32 33 7l l4 2 5 ll) 15 20 3 5 208 63 592 33 32 70 l7 I0 222 77 S48 29 32 7| l3 i5 222 523 24 32 7O 14 89 20 216 85 SI 21 32 7l l3 Properties of the vulcanized mixtures vulcanization tem erature: 150C. Mixture VZ F M 300 1 15 101 50 635 53 45 64 13 3O 99 66 483 36 42 67 6 45 96 65 490 34 40 66 6 268 60 94 64 480 34 40 67 9 2 15 154 137 335 I8 45 67 8 30 146 v 138 307 13 44 68 45 145 138 305 10 43 68 5 210 60 147 143 303 11 42 67 5 M 200 3 15 125 77 440 22 42 66 8 30 125 I01 287 I4 41 69 5 45 125 102 262 10 40 69 5 223 60 I29 104 293 14 39 69 4 In examples 3 to 5 there were used rubber mixtures Example 6 based on styrene-butadiene copolymers which contained as silicious fillers synthetic aluminum silicate or Recipe: Mixture Mixture precipitated silica or a natural silicate (colloidal ka- 1 2 olin). As organo-silane reinforcing additives there were Butadiene ac,y|onmi|e wbbe, employed bi's-[3-triethoxysilyl propyl]-tetrasulfide or (Perbunan N 3310 f F r nfa r n b' [3 tr eth s'l I re l] disulfide' these were Bayer AG) 1S 1m Y P py Pyrogenic silica (Aerosil 130 V compared with the 3-mercaptopropyl trimethoxy s1lane Z of DEGUSSA) 40 40 inc oxide 4 4 of the prior art in otherwise 1dent 1cal mixtures. Bis [3 triethoxysilyl propyl1 According to examples 3 and 4 it was not possible to -mtrasumde L5 produce kneader mixtures with 3-mercaptopropyl tri- X Drphenylguamdme L5 1 .5 methoxysflane without premature scorching while thrs Sulfur 275 N5 presents no problem with the rubber mixtures containing the polysulfideorganosilanes of the invention. 30

In comparison with the respective standard mixtures Mixing Procedure without silane additive the vulcanization properties of Premixing in a kneader at 80C. flow temperature. .the new rubber mixtures are clearly better. Tensile strength and modulus are increased, the remaining; e longanon after break was reduced and the DIN abra- 1 Additive or Treatment Ended After SlOIl lmproved.

Example 5 shows that this effect occurs even in the Butadiene-acrylonitrile-rubber 0 minutes k amount of silica, stearic acid 1 minute addit on of a relatively inactive sllicate tiller such as yambumofsmcazinc oxide colloidal kaolin. organosilane 2.5 minutes Example 5 also demonstrates with reference to the 40 Ram hfted and Sweptdown 4 minutes Batch dumped 4.5 minutes properties of the unvulcanized mixtures the clear advance of the present invention over the prior art compound (3-mercaptopropyl trimethoxysilane in that the 5 l prior art compound increases the values for DH/DE: After 24 hours storage the mixing 1n the kneader at and ML 4 and it drastically shortens the scorch time I 1 flow through ten'lpel'amfe was completed ON the contrary in the new rubber mixtures the values g tlme DH/DE and ML 4 are changed in a positive direction while the Mooney-scorch time t is not substantially different from that of the comparison mixture without any I 50 properties of the vulcanized mixtures silane additive. Mixture 1 Mixture 2 The following examples 6 to 9 illustrate the fact that 350 26 1950 31 the new rubber mlxtures also can be produced w1th 1 gH/DE equally good success based on butadiene -acrylonitrile its ML 4 132 polymers, butyl rubber, polychloroprene rubber or L2! L2] ethylenepropylene-terpolymer. WM

Properties of the vulcanized mixtures vulcanization temperature: C.

ZF M 200 Example 7 W Example 8- Continued Recipe: Mixture Mixture 2 5 Recipe: Mixture Mixture Butyl rubber l l00 2 Finely divided, precipitated silica (LlLTRASlL VN 3 of Degussa) 50 50 Di o to|y|guanidine Zmc 5 5 Magnesiumoxide 4 4 Steam 1 l Stearic acid I l plfsticizq (petrlleum 5 5 Mixture of liquid 'andplastie Bis-l3-triethoxysilyl-propyl] l0 parafi-ms (vasehhe) 1 1 'tcmlsulfide Phenyl- -naphthylamine (anti- Z-Mereaptobenzothtazole l l oxidant) 2 2 Tetramethyliuramdisulfide 0.5 0.5 Finely divided precipitated silica (ULTRASIL VN .2 of DEGUSSA) so so Plasticizer l 5 (nzgphtheirliie 'hyldII'OCHI'bOHS) l0 Bis- -triet ox si r0 Mlxmgiafocejdure -tiatrasultide y p py] 1.5

Premixmg in the kneader at 60C flow temperature. 2-mercaptoimidazoline 0,75 0.75

Zinc oxide 5 5 2O Additive or Treatment Ended After Butyl rubber 0 minutes $6 amount of silica, stearic acid 2 minutes Mlxmg F o 9% amount of silica, zinc oxide, Premixmg m the kneader at 60 C. flow temperature.

organosilane, plasticizer 4 minutes Ram lifted and swept down 6 minutes M Batch dumped 7 minutes Additive or Treatment Ended After The final mixing took place on an open mill at 50C. P I l b v roll temperature o ych oro utadiene. guamdme derivate 0 minutes Antioxidant, magnesium oxide Stearic acid, vaceline, A: of the amount I minute Additive or Treatment Ended After onhe S'hca A of the amount of the silica, k the Batch q 0 minutes amount of the plasticizer, organosilane 12.5 minutes Cut in twice right and left lv m nute Accelerator andhsulfur f 3 minutes the amount of the Sihca 1, the Cut in twice rig t and le t minutes t h I Mixture sheet pulled off 5 minutes dmmm of e plmlcwer Ram lifted and swept down -4 minutes 40 Removal and cooling 5 minutes in awaterbath l '5 minutes Properties of the unvulcanized mixtures Mixture l Mixture 2 PH/DE 2% 45 After 24 hours storage there was mixed in thekneader a; 40 1726 at C flow temperature the Z-Merkaptoimidazoline M 4 l5 l5 and the zinc oxide and there was 5 minutes cooling in the waterbath.

Properties of the vulcanized mixtures vulcanization temperature: 160C. Mixture VZ Z M 300 BD bl.D. E SH EF A l l() 85 19 893 100 I2 64 15 20 103 23 850 100 I3 67 16 40 H7 27 818 I00 I3 68 23 60 1 l6 28 795 96 I3 70 25 270 H2 28 778 93 l3 7O 26 2 l0 I08 27 805 97 ll 63 I7 20 I33 34 773 78 ll 64 22 40 l45 40 738 68 12 67 23 60 148 43 708 64 12 69 28 227 80 15] 45 693 63 l2 69 27 Example 8 Properties of the unvulcanized mixtures Mixture l Mixture 2 Recipe: Mixlture Mixzture DH/DE t, 6.2 Polychlorobutadiene rubber I00 100 :61 4 2 I (Baypren 210 of Farbenfabriken 1 42 l 42 Bayer, AG, Leverkusen) sp. gr.

Properties of the \ulcani7cd mixtures Mixture V7. Z1" M 300 lid NJ). 1- SH iii" A 1 I 156 47 810 la 34 57 .17

20 1m 52 790 ix 33 e1 31 30 171 53 742 17 33 62 23 161 40 171 53 735 l 33 62 l) Example 9 lroperties of the vulcanized mixtures Mixture Mixture 15 Vaulcanization temperature: 160C. Recipe: i l 2 Mi M Tcrpolymcr ethylcnc pmpylenc I ture vz ZF 300 BD bLD. E SH EF rubber (Keltan of DSM) 100 1 IO 67 23 r 825 43 4O 53 7 Finely divided, reci itatcd 20 20 62 29 627 25 42 57 i 3 5111011 (EXTRUs iL o DEGUSSA) mp 100 55 32 42 59 2 Naphthenie hydrocarbon as 2 1O 77 42 725 26 4] 54 8 so so 38 31 i: is?) z :2 22 2 Titandioxide l0 10 25 Zinc oxide 5 5 I In example 6 there was used a rubber mixture formu- Slcflrlc acld l l lated according to the invention based on a nitrile rub- Bisil3 triethoxylsflyl propyl1 ber which contained as the siliceous fillera pure silica -tctrasulfide 5 30 produced by flame hydrolysis (Aerosil V of Tetrammhyhhiummdisumdc 0'8 08 Degussa) and to which was added bls-[3-tr1ethoxys1lylprOpyH-tetrasuIfide as the organosilane reinforcing ad- Dimcthyldiphcnylthiuramdisulfide 1.5 1.5 ditive, Telluriumdicthyldithioearbamate 0.8 0.8 The m Yiscosity mixture 2 of Exampl? 6 is 35 clearly reduced in comparison to the standard mixture D'pemamethylcncthurammmsulfidc 03 08 without organosilane addition. This signifies a reduced S lf lo 20 expenditure of energy and a lower cost in the further working of the raw mixture; the scorching time t is I only shortened unsubsta'ntially. The vulcanizate of Mix- Mixing Procedure 40 ture 2 shows a significant improvement in regard to Premixing in the kneader at 80C. flow temperature.

After 24 hours storage the mixing was finished in the kneader at 80C. flow temperature (Mixing time 1.5. minutes).

Properties of the unvulcanized mixtures Mixture 1 Mixture 2 DH/DE 550/ 400/ t 8.5 19.2

t 16.4 50.4 ML 4 50 40 sp. gr. 1.16 1.16

tensile strength, modulus and DIN-abrasion when it is compared with comparison mixture 1 without organosilane addition.

According to example 7 the rubber mixture of the invention was based on butyl rubber containing a precipitated silica (Ultrasil VN 3 of Degussa) as the siliceous filler and the bis-[3triethoxy-silyl propyl]-tetrasulfide as the organosilane reinforcing additive.

This addition of organosilane did not lead to premature scorching of the already very sharply accelerated standard mixture, but instead surprisingly to an increase in the Mooney-scorch time t Tensile strength, modulus and remaining elongation of the vulcanizate were clearly better in comparison to the vulcanizate from the standard mixture.

Example 8 describes a rubber mixture based on a polychloroprene rubber with a precipitated silica (Ultrasil VN 3 of Degussa) as the siliceous filler and again using the bis-[3-triethoxysilyl propyl]-tetrasulfide as the organosilane reinforcer for cross-linking. The

scorching behaviour of Mixture 2 is practically unmore than 60 kp/cm higher. The latter indicates an improvement of about 100 percent or more based on the Mixture l devoid of the organosilane.

Example 9 concerns a rubber mixture based on an Step 2 Final mixing in the kneader-at 80C flow temperature. Accelerator and sulfur are mixed in in the kneader Mixing time 1.5 minutes.

ethylene-propylene nonconjugated diene-terpolymer 5 with a further precipitated silica (Extrusil of Degussa) P l f I as the siliceous filler and the bis-[3-triethoxysilyl mpemes o the "vulcamzed m'xmres propyl l-tetrasulfide as the organosilane. Also in this Mixture] MixtureZ case there is produced a surprising increase in the t5 0 18 l scorch time ML 4 is reduced about Mooney i0 {35 5 units, both in comparison to the standard mixture-with- ML 4 67 67 sp. gr. l.l9- Ll) out organosilane. The properties of the vulcanizate Properties of the vulcanized mixtures vulcanization temperature: 160C.

Mixture VZ ZF M 300 BD bl.D. E SH- .EF A

from Mixture 2 formulated according to the invention Example 1 1 clearly exceed those of Mixture 1 without silane in regard to tensile strength, modulus and remaining elonga- Earth-Mover" Tire tread mixture tion after break. Mixture Mixture 7 Example 10 Real) Natural rubber Passenger automobile tire tread mixture (Ribbed Smoked Sheets l) l()() lOO Mixture Mixture Pentachlorthiophenyl-zinc salt Recipe 1 2 3O (Renacit IV of Farbenfabriken Bayer, Leverkusen) 0.25 0.25 Oil extended styrene hutudicnc rubber lSAF-LM Carbon black (Bunu Huls l7l2) 96.5 96.5 (CORAX 6 LM of Degussa) 6O cis-l.4-Polybutadiene Mixture of IO parts of bis[3- (Buna CB 10) 3O 30 triethoxysilyl-propyl]-tetrasulfide and lOO parts of Finely divided precipitated precipitated silica (ULTRASlL silica (ULTRASlL VN 3 of DEGUSSA 75 7O VN 30f Degussa) 66 Bis-l3-triethoxysilyl-propyl]- Zinc oxide 5 5 tetrasulfide v5 4O Stearic acid 2.5 2.5 Mixture of equal parts of precipitated silica (ULTRASIL VN 3) Antioxidant, phenyl-aand Bis-[3-triethoxysilyl-propyl] naphthylamine l l -tetrasulfide 10 Antioxidant hen l-B- Zinc oxide 4 4 naphthylamii ie y l l Steanc acid 12 Antioxidant N-lsopropyl- 0 8 O 8 N- h lh l d' Plasticizer (naphthenic p eny p p any en lamme hydrocarbons) l5 Rubber-ocozerite (Protektor 3888 W h Antioxidant, phenyl-B-naphthylgie i c iie g ifi l'h S amine 1.5 1.5

- Plasticizer (naphthenic Antioxidant, N-lso-propyl-N'- v 2 3 phenyl-p-phenylene-diamine 1.5 1.5 hydrocarbon) Benzthiazolyl-2-cyclohexylsulgi i gii q iifl igi igzit 0.6 fcnamide L2 1.2

Diphenylguanidine 3.5 3.5 Diphenylguamdme 2 Sulfur 1.6 1.6 12

Mixing Procedure: Up-side-down Premixing in the Kneader at 80C. flow temperature Additive or Treatment Ended-After Step l Fillers, chemicals, polymers 0 minutes Ram lifted and swept down 3 minutes Batch dumped 3.5 minutes Storage 24 hours Mixing Procedure: Up-side-down Premixiiig in the kneader at C. flow temperature Step 2:

Final mixing in the kneader at 80C. flow temperature. Accelerator and sulfur are mixed in in the kneader Mixing time 1.5 minutes invention in comparison to the standard mixture which is altogether a desired effect since it leads f.i. to a reduction in the production costs for the tire manufacturer.

In the vulcanization properties which in general correspond to those of the standard mixture there are two Propertles ""vulcamzed m1xtures properties in which the mixture of the invention stands Mixture l Mixture 2 out; the clearly increased resistance to tear propagation M S h 25 4 l9 9 and the reduced heat build up. The resistance to tear 632 propagation is increased 35 percent in comparison to Mooney Viscosity ML4 88 77 the carbon black remforced standard (or reference) H8 mixture, the heat bui ld up is lowered about 31 percent,

Properties of the vulcanized mixtures vulcanization temperature: l45C.

Mixture vZ ZF M 300 BD E I SH EF A T (0.250") According to Example 10 a passenger automobile from 87 to 64C. In the evaluation of the absolute valr tread recipe n according to mpl 11 ues of the Goodrich Flexometer test it should be oban earth mover tire tread recipe are disclosed and used. served th t thi wa a r d with a stroke of 0.250 As reinforcing additive for both recipes h r r inch, while ASTM prescribes a stroke of 0.175 inch. It Used -l y y p py li fOr the is especially noteworthy that the DIN abrasions of the PKW tire tread m the form Of a mlXture Wlth $11168 carbon black mixture and ofthe silica mixture are practhe ratio 1:1 and for the earth mover tire tread in the i ll h Same form of a mixture with finely divided silica in the ratio I was l a i fi d h b use f h 1110- ganosilane reinforcing additive of the invention that for Example 9 Shows e t the range of error of e the first time it is possible to easily produce practical rubber teehhlqhe thvestlgatthg h h used there was m1xtures w1th only s1l1ca or s1l1ceous filler and then to h e e e between the pp h Ohthe rethfete' vulcanize which products in the sum of their properties t adfhtlve h P e form and the apPheatleh 0f the e are equal to correspondmg carbon black filled m1xtures c j ah h i t 1h ch ie ofa hhxtute Wlth P P and even exceed the carbon black m1xtures 1n dec1s1ve tate y tsperse S1 characteristics.

The Properties of the hhvuteehtzed and the e The rubbers disclosed above are all curable, e.g., nized m1xtures show one sk1lled 1n the art that by us1ng with lf or other Curing (vulcanizing) agents the reinforcing additive of the invention there are im- 40 The compositions f the invention can Consist f or Pe to a great extent the shlea rehtfoteed PKW consist essentially of the siliceous filler and the orthe trettd m1xtures prepettles Whteh eertespehd to the ganosilane or the composition can consist of or consist Propetttee of correspqndmg clarboh black mlxtureessentially of these components with the other material Also, for the first tlme, 1t 15 poss1ble by use of the mentioned polysulflde funct1onalorganos1lane re1nforc1ng add1t1ve to produce silica reinforced PKW tire tread mixtures without change of the previously customary mixing and 1 E mple vulcanization processes in the rubber industry, which mixtures in all industrial applications have characteris- Itailcs l\ivhichfare alt least equal to corresponding carbon passenger Tire Tread Mixwm ac rem orce m1xtures. In Example 11 the reinforcing additive of the inven- Recipe tion in a silica reinforced Earth-Mover tire treadmixture is compared with a conventional carbon black ret n Styrenebutad1ene rubber 1nforcecl Earth-Mover tread m1xture. (Bum, U15 1712) 965 965 In Example 1 1 it is proven that by using the additives of the invention there are imparted such properties to g 30 30 silica reinforced rubber mixture which in decisive Carbon Black ISAF points exceed those of carbon black remforced m x (Com 60f DEGUSSA) 75 37's utres; for example 1n regard to tear propagation reslstance and the heat build up (Heat build-up Goodrich F n y divided Precipitated Flexometer Test). s1l1ca (ULTRASIL VN 3 of DEGUSSA) 35 In comparison to the standard Mixture 1 it is estab- Mixtureof equal parts of precipilished that by use of the reinforcing additive of the in- 3) and vention the Mooney-scorch and Mooney cure time are tetrasulfide 5 somewhat shortened but they still remain in a range Zmc ox1de v 4 4 suitable for 1ndustr1al practice. The raw m1xture VISCOS- V ity is 11 Mooney units lower in the composition of the Stearic acid Example l2-Continued Passenger Car Tire Tread Mixture Mixing Procedure: Up-side-down Premixing in a kneader at 80C. flow temperature Additive or Treatment Ended-After Step 1 Fillers, chemicals, polymers minutes Ram lifted and swept down 3 minutes Batch dumped 3.5 minutes Storage 24 hours Step 2 Final mixing in the kneader at 80C. flow tempera- R R 1 1 (1) -Si R1 (2) -Si R2 s R s R s 2 0 mm or (3) -Si 2 wherein R, is alkyl of 1 to 4 carbon atoms, cyclohexyl or phenyl and R is alkoxy of 1 to 8 carbon atoms, cy-

cloalkoxy with 5 to 8 carbon atoms or alkylmercapto with 1 to 8 carbon atoms, alk is divalent hydrocarbon of 1 to 18 carbon atoms, n is a number of 3.0 to 6.0, a siliceous filler and a curable rubber polymer, the organosilane being present in an amount of 0.1 to 50 20 parts per 100 parts of polymer and the siliceous filler being present in an amount of 10 to 250 parts per 100 parts of polymer.

2. A composition according to claim 1 wherein n is a number of 3.0 to 4.0.

3. A composition according to claim 2'where Z is (3 R is ethoxy and alk is alkylene of 2 to 4 carbon atoms.

4. A composition according to claim 2 wherein the siliceous material is kaolin.

5. A composition according to claim 2 wherein the siliceous material is aluminum silicate.

6. A composition according to claim 2 wherein the polymer is butyl rubber.

E fsll l i d are m'xed m m the 7. A composition according to claim 2 wherein the nedderminutes polymer is ethylene-propylene non-conjugated polyene terpolymer. I Properties of the unvulcanized mixtures A accplidmg to i i the siliceous filler 1S finely divided precipitated sillca or py- Mixture 1 Mixture 2 rogenic silica. i. 2L7 202 9. A composition according to claim 2 wherein Alk ip. g9 is a saturated aliphatic hydrocarbon, unsaturated a11- Ml. 4 ,4 my H6 H8 phatic hydrocarbon or cylcoaliphatic hydrocarbon group.

Properties of the vulcanized mixtures vulcanization temperature: 160C.

Mixture VZ ZF M 300 Ed E SH EF A T "(stroke 0 250 inches) Example 12 shows that the organosilanes containing rubber mixtures of the invention may contain advantageously as active filler both silica and carbon black. The properties of both unvulcanized rubber mixtures (1) and (2) are practically the same and show the expert that the silica containing rubber mixture can be used on a large-scale production of tires as well as the carbon black containing rubber mixtures of the prior 60 art.

The properties of the vulcanized mixture containing silica and carbon black show clearly better values in tensile strength, rebound, resistance to tear propaga- 10. A composition according to claim 9 wherein Alk has 1 to 6 carbon-atoms.

55 11. A composition according to claim 10 wherein Alk is a saturated aliphatic hydrocarbon group of 2 to 4 carbon atoms.

12. A composition according to claim 11 wherein Z is (3).

13. A composition according to claim 12 wherein Alk has 3 carbon atoms and all R groups are alkoxy of 1 to 4 carbon atoms.

14. A composition according to claim 12 wherein Alk is a saturated aliphatic hydrocarbon group of 2 to tion and heat build-up on dynamic stress than the vul-. 3 carbon atoms and all R groups are ethoxy.

canized mixture containing only carbon black.

What is claimed is:

1. A composition comprisng an organosilane having the formula AalkS,,alkZ, in which Z is 15. The product obtained by curing the composition of claim 2.

16. A composition according to claim 2 wherein the polymer isa polymer of a conjugated diene.

1 organosilane 17. A composition according to claim 2 wherein the polymer is natural rubber, polybutadiene, polyisoprene, butadiene-styrene copolymer, butadieneacrylonitrile copolymer, polychlorobutadiene, butyl rubber, chlorobutyl rubber, bromobutyl rubber or ethylene-propylene non-conjugated polyene terpolymer.

18. A composition according to claim 17 wherein the polymer is a sulfur curable polymer and the composition includes sulfur.

19. The product obtained by curing the composition of claim 18.

20. A composition accirding to claim 18 wherein the siliceous material is silica, kaolin or aluminum silicate.

21. A composition according to claim 20 wherein the compound comprises 3,3 -bisltriethoxysilyl propyl]-tetrasulfide.

22. A composition according to claim 2l'wherein the siliceous material is silica.

23. A composition according to claim 12 wherein the siliceous material is silica, kaolin or aluminum silicate.

24. A composition according to claim 23 wherein the siliceous material is silica.

25. A composition according to claim 24 wherein the silica is finely divided pyrogenic silica.

26. A composition according to claim 25 wherein the organosilane compound comprises 3,3-bis- [triethoxysilyl propylltetreasulfide.

27. A composition according to claim 1 wherein the organosilane has the formula R I R I l I I R s1 Alk s Alk Si R, 2 z

where R is alkoxy of l to 3 carbon atoms, Alk is alkylene of 2 to 5 carbon atoms and n is 3.0 to 4.0.

ozone stabilizer. 

1. A COMPOSITION COMPRISING AN ORGANOSILANE HAVING THE FORMULA A-ALK-SN-ALK-Z, IN WHICH Z IS
 2. A composition according to claim 1 wherein n is a number of 3.0 to 4.0.
 3. A composition according to claim 2 where Z is (3), R2 is ethoxy and alk is alkylene of 2 to 4 carbon atoms.
 4. A composition according to claim 2 wherein the siliceous material is kaolin.
 5. A composition according to claim 2 wherein the siliceous material is aluminum silicate.
 6. A composition according to claim 2 wherein the polymer is butyl rubber.
 7. A composition according to claim 2 wherein the polymer is ethylene-propylene non-conjugated polyene terpolymer.
 8. A composition according to claim 2, wherein the siliceous filler is finely divided precipitated silica or pyrogenic silica.
 9. A composition according to claim 2 wherein Alk is a saturated aliphatic hydrocarbon, unsaturated aliphatic hydrocarbon or cylcoaliphatic hydrocarbon group.
 10. A composition according to claim 9 wherein Alk has 1 to 6 carbon atoms.
 11. A composition according to claim 10 wherein Alk is a saturated aliphatic hydrocarbon group of 2 to 4 carbon atoms.
 12. A composition according to claim 11 wherein Z is (3).
 13. A composition according to claim 12 wherein Alk has 3 carbon atoms and all R2 groups are alkoxy of 1 to 4 carbon atoms.
 14. A composition according to claim 12 wherein Alk is a saturated aliphatic hydrocarbon group of 2 to 3 carbon atoms and all R2 groups are ethoxy.
 15. The product obtained by curing the composition of claim
 2. 16. A composition according to claim 2 wherein the polymer is a polymer of a conjugated diene.
 17. A composition according to claim 2 wherein the polymer is natural rubber, polybutadiene, polyisoprene, butadiene-styrene copolymer, butadiene-acrylonitrile copolymer, polychlorobutadiene, butyl rubber, chlorobutyl rubber, bromobutyl rubber or ethylene-propylene non-conjugated polyene terpolymer.
 18. A composition according to claim 17 wherein the polymer is a sulfur curable polymer and the composition includes sulfur.
 19. The product obtained by curing the composition of claim
 18. 20. A composition accirding to claim 18 wherein the siliceous material is silica, kaolin or aluminum silicate.
 21. A composition according to claim 20 wherein the organosilane compound comprises 3,3''-bis-(triethoxysilyl propyl)-tetrasulfide.
 22. A composition according to claim 21 wherein the siliceous material is silica.
 23. A composition according to claim 12 wherein the siliceous material is silica, kaolin or aluminum silicate.
 24. A composition according to claim 23 wherein the siliceous material is silica.
 25. A composition according to claim 24 wherein the silica is finely divided pyrogenic silica.
 26. A composition according to claim 25 wherein the organosilane compound comprises 3,3-bis-(triethoxysilyl propyl)-tetreasulfide.
 27. A composition according to claim 1 wherein the organosilane has the formula
 28. A composition according to claim 27 including sulfur, accelerator and the curable rubbery polymer is at least one member of the group consisting of natural rubber, butadiene-styrene copolymer, cis-1,4-polyisoprene, butadiene-acrylonitrile copolymer, polybutadiene, polychlorobutadiene and ethylene-propylene-non-conjugated polyene terpolymer.
 29. The product by curing the composition of claim
 28. 30. A composition according to claim 2 including a rubber reinforcing carbon black.
 31. A composition according to claim 30 including sulfur, accelerator, processing oil, light stabilizers and ozone stabilizer. 